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CORTRAK ENTERAL ACCESS DEVICE, MODEL 20-0900

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091637
510(k) Type
Traditional
Applicant
CORPAK MEDSYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2009
Days to Decision
117 days
Submission Type
Statement